Cas 126166-65-2,Methanesulfonic acid 2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-ethyl ester

126166-65-2

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Basic information

Product Name: Methanesulfonic acid 2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-ethyl ester
Synonyms:
CAS NO:126166-65-2
Molecular Formula:
Molecular Weight: 416.496
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Methanesulfonic acid 2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid 2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-ethyl ester(126166-65-2)
EPA Substance Registry System: Methanesulfonic acid 2-((S)-3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-ethyl ester(126166-65-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 126166-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126166-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126166-65:
(8*1)+(7*2)+(6*6)+(5*1)+(4*6)+(3*6)+(2*6)+(1*5)=122
122 % 10 = 2
So 126166-65-2 is a valid CAS Registry Number.

126166-65-2Upstream product

126166-65-2Downstream Products

126166-69-6 (S)-1-bromo-2-((S)-O-benzyl-N-tert-butoxycarbonylserylamino)ethane

126166-65-2Relevant academic research and scientific papers

The Chemical Conversion of C-Terminal Glycines in Peptides into Taurine

Higashiura, Kunihiko,Toyomaki, Yoshio,Ienaga, Kazuharu

, p. 521 - 522 (2007/10/02)

The first chemical conversion of C-glycine in dipeptides into taurine has been achieved using a general substitution of a sulpho group for a halogeno or mesyl group via the corresponding amino acid 2-halogenoethyl- or 2-methanesulphonyloxyethyl-amides, ea

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